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Folate Functionalized and Evodiamine-Loaded Pluronic Nanomicelles for Augmented Cervical Cancer Cell Killing

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dc.contributor.authorSolanki, Raghu-
dc.contributor.authorJangid, Ashok Kumar-
dc.contributor.authorJadav, Mahima-
dc.contributor.authorKulhari, Hitesh-
dc.contributor.authorPatel, Sunita-
dc.date.accessioned2024-08-08T10:02:17Z-
dc.date.available2024-08-08T10:02:17Z-
dc.date.issued2023-09-
dc.identifier.issn1616-5187-
dc.identifier.issn1616-5195-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/21378-
dc.description.abstractEvodiamine (Evo) is a natural, biologically active plant alkaloid with wide range of pharmacological activities. In the present study Evo-loaded folate-conjugated Pluronic F108 nano-micelles (ENM) is synthesized to enhance the therapeutic efficacy of Evo against cervical cancer. ENM are synthesized, physicochemically characterized and in vitro anticancer activity is performed. The study demonstrates that ENM have nanoscale size (50.33 +/- 3.09 nm), monodispersity of 0.122 +/- 0.072, with high drug encapsulation efficiency (71.30 +/- 3.76%) and controlled drug release at the tumor microenvironment. ENM showed dose-dependent and time-dependent cytotoxicity against HeLa human cervical cancer cells. The results of in vitro anticancer studies demonstrated that ENM have significant anticancer effects and greatly induce apoptosis as compared to pure Evo. The cellular uptake study suggests that increased anticancer activity of ENM is due to the improved intracellular delivery of Evo through overexpressed folate receptors. Overall, the designed ENM can be a potential targeted delivery system for hydrophobic anticancer bioactive compound like Evo.-
dc.language영어-
dc.language.isoENG-
dc.publisherWiley-VCH GmbH-
dc.titleFolate Functionalized and Evodiamine-Loaded Pluronic Nanomicelles for Augmented Cervical Cancer Cell Killing-
dc.typeArticle-
dc.publisher.location독일-
dc.identifier.doi10.1002/mabi.202300077-
dc.identifier.scopusid2-s2.0-85159651229-
dc.identifier.wosid000991469700001-
dc.identifier.bibliographicCitationMacromolecular Bioscience, v.23, no.9-
dc.citation.titleMacromolecular Bioscience-
dc.citation.volume23-
dc.citation.number9-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPolymer Science-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.subject.keywordPlusCYTOCHROME-C-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusPATHWAYS-
dc.subject.keywordPlusDELIVERY-
dc.subject.keywordPlusRELEASE-
dc.subject.keywordPlusINJURY-
dc.subject.keywordAuthorcervical cancer-
dc.subject.keywordAuthordrug delivery-
dc.subject.keywordAuthorevodiamine-
dc.subject.keywordAuthorfolate targeted nanomedicine-
dc.subject.keywordAuthorfunctionalized polymers-
dc.subject.keywordAuthorpluronic F108 nanomicelles-
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